Explore all the ways you can support others with axial SpA by fundraising for NASS. You can become a regular donor, pledge to leave a gift in your will to NASS, organise your own fundraiser, take on a challenge event, join a community fundraiser, donate whilst shopping online – and much more!
Whatever you choose to do, every penny you raise will help support people affected by the condition. Browse through the options below!
From 1-30 September, Yoga for AS and NASS will be partnering to deliver free strength-training and stretching classes to everyone taking part, to move more for your axial SpA, channel your inner-strength and help us raise vital funds for people affected by the condition.
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If you have your own ideas on how to raise funds for NASS, Go Orange for AS and we will help you set up your event and support you along the way!
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If you are planning on celebrating Halloween this year, why not turn it into a fun fundraiser?
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Chris signed up to the NASS Lottery as a way to support people living with axial SpA. In May, he won the £2,000 2nd prize! Read Chris' story.
Chris' story
“I think it is important that we all do our bit to keep NASS information and help available for ourselves and each other.”
Ronan's story
Find out more about Charlie's story living with axial SpA and why he has written a book to raise awareness and funds for people affected by the condition.
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Browse through all the events taking place across the UK which you can sign up to and raise funds for NASS.
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Take a look at the extensive list of ultra challenges that you can take on abroad or in the UK to raise funds for NASS.
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Do you want to go on an unforgettable adventure whilst also raising funds for people living with axial SpA? Check out what's going on around the world!
Find out moreHost a barbecue or garden party, sell your items or bake some goods for your friends, family and neighbours and help raise funds for people living with axial SpA!
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Create a quick and easy online raffle or auction and invite your friends and family to take part to help raise funds for NASS!
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Interested in exploring a partnership with NASS? We believe that Corporate Social Responsibility should be a shared endeavour that creates value for both sides. From supporting employee mental health and designing challenge events, to providing team building opportunities and corporate entertainment experiences, we would be delighted to discuss how we might assist you.
Contact Paul at NASS
Find out why your support really does matter, the impact that you can have, and why your help has never been more urgent.
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Watch and read the stories of those who have raised vital funds to support others with axial SpA.
Read moreIf you have any questions about fundraising for NASS, please don't hesitate to email fundraising@nass.co.uk or call 020 8741 1515 (press option 2)
1 in 200 of the adult population in the UK have axial SpA (AS). That's twice as many as multiple sclerosis and Parkinson's disease.
Axial SpA (AS) is a condition that affects young people. Symptoms start late teens to early twenties, with the average age of onset being 26.
The current average delay to diagnosis from when symptoms start is 8.5 years, by which irreversible damage to the spine may have occurred.
59% of people with axial SpA (AS) report experiencing mental health problems compared to 25% of those with musculoskeletal conditions overall.